Visitor Monitoring Drug History: FEMCON FE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: FEMCON FE
FDA Application No: (NDA) 021490
Active Ingredient(s): ETHINYL ESTRADIOL; NORETHINDRONE
Company: WARNER CHILCOTT
 
Label History
 
View the label approved on February 2, 2007 for FEMCON FE, (NDA) 021490


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/29/2007 005Control Supplement Letter
Label 
11/14/2003 000Approval Letter
Label
Review 
 
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